Services Medical Devices Quality Management and Training

Quality Management and Training

An effective QMS for the lifecycle stage of your product is vital to ensuring safety and quality of your medical device.

At DLRC, our consultants have the expertise to ensure that you meet stringent global quality requirements such as the US FDA Quality System Regulation (QSR), EU Medical Device Regulation, ISO 13485 and MDSAP (Australia, Brazil, Canada, Japan and US).

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